FDA Inspection 748094 — Hi-Dow International Inc

Hi-Dow International Inc — FEI 3003895865

The FDA completed an inspection of Hi-Dow International Inc on September 21, 2011 in Maryland Heights, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Maryland Heights, MO (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures